| Literature DB >> 34224109 |
Jing Zhang1,2, Kui Ma1, Xiangyu Wang2, Yinbo Jiang3, Shan Zhao2, Junxian Ou2, Wendong Lan2, Wenyi Guan2, Xiaowei Wu2, Heping Zheng3, Bin Yang3, Chengsong Wan2, Wei Zhao2, Jianguo Wu4, Qiwei Zhang5,6.
Abstract
Human adenovirus type 55 (HAdV-B55) is a re-emergent acute respiratory disease pathogen that causes adult community-acquired pneumonia (CAP). Previous studies have shown that the receptor of HAdV-B14, which genome is highly similar with HAdV-B55, is human Desmoglein 2 (DSG2). However, whether the receptor of HAdV-B55 is DSG2 is undetermined because there are three amino acid mutations in the fiber gene between HAdV-B14 and HAdV-B55. Here, firstly we found the 3T3 cells, a mouse embryo fibroblast rodent cell line which does not express human DSG2, were able to be infected by HAdV-B55 after transfected with pcDNA3.1-DSG2, while normal 3T3 cells were still unsusceptible to HAdV-B55 infection. Next, A549 cells with hDSG2 knock-down by siRNA were hard to be infected by HAdV-B3/-B14/-B55, while the control siRNA group was still able to be infected by all these types of HAdVs. Finally, immunofluorescence confocal microscopy indicated visually that Cy3-conjugated HAdV-B55 viruses entered A549 cells by binding to DSG2 protein. Therefore, DSG2 is a major receptor of HAdV-B55 causing adult CAP. Our finding is important for better understanding of interactions between adenoviruses and host cells and may shed light on the development of new drugs that can interfere with these processes as well as for the development of potent prophylactic vaccines.Entities:
Keywords: Adenovirus receptor; Desmoglein 2 (DSG2); Human adenovirus type 55 (HAdV-B55); Severe community-acquired pneumonia
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Year: 2021 PMID: 34224109 PMCID: PMC8692558 DOI: 10.1007/s12250-021-00414-7
Source DB: PubMed Journal: Virol Sin ISSN: 1995-820X Impact factor: 6.947